Caplugs/Evergreen
CAPlugs · Model 240-3007-L60 · UDI-DI 00810044201475
0
510(k) clearances
28
Adverse events
4
Recalls
328
Facilities
Description
7 mL Transport Vials with Caps
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-09 | Milestone S.R.L. | There is a possibility of reagent leakage from the specimen container. |
| 2021-12-01 | MEDLINE INDUSTRIES, LP - Northfield | Product stored incorrectly in temperature controlled setting instead of refrigeration. |
| 2016-03-03 | Dynarex Corporation | Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton. |
| 2011-02-18 | Cardinal Health Inc | In one lot of product (lot# 1091745), the label for the small version of the sock (catalog number 65652-123) was improperly used for the larger version of the product (65652-124) |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.